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68523003: Cerebral white matter structure (body structure)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
113807010 Cerebral white matter en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
501040012 Cerebral white matter structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
808368013 Cerebral white matter structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
113807010 Cerebral white matter en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
113807010 Cerebral white matter en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
501040012 Cerebral white matter structure en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
501040012 Cerebral white matter structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
808368013 Cerebral white matter structure (body structure) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
808368013 Cerebral white matter structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


140 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cerebral white matter structure Is a Cerebral hemisphere white matter part false Inferred relationship Existential restriction modifier (core metadata concept)
Cerebral white matter structure partie de Entire cerebral hemisphere false Additional relationship (core metadata concept) Existential restriction modifier (core metadata concept)
Cerebral white matter structure partie de Entire brain and spinal cord (body structure) false Additional relationship (core metadata concept) Existential restriction modifier (core metadata concept)
Cerebral white matter structure Is a White matter structure of brain and spinal cord (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Cerebral white matter structure Is a Structure of telencephalon (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Cerebral white matter structure Is a Cerebral hemisphere part true Inferred relationship Existential restriction modifier (core metadata concept)
Cerebral white matter structure Laterality Side true Inferred relationship Existential restriction modifier (core metadata concept)
Cerebral white matter structure Is a Layer of cerebrum true Inferred relationship Existential restriction modifier (core metadata concept)
Cerebral white matter structure Is a Structure of white matter of brain true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Leukoencephalopathy due to copper deficiency Finding site True Cerebral white matter structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Cathepsin A-related arteriopathy, strokes, leukoencephalopathy Finding site True Cerebral white matter structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Silent white matter disease due to vascular disease Finding site True Cerebral white matter structure Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare genetic neurological disorder characterized by infantile onset of progressive leukoencephalopathy, microcephaly, severe global developmental delay, and spasticity resulting in quadriparesis and posture deformation. Additional features include an abnormally exaggerated startle reflex, seizures, dystonia, and hypomimia or amimia, as well as progressive chest deformities and contractures of large and hyperextensibility of small joints, among others. Thin corpus callosum is a prominent feature in brain imaging, in addition to white matter abnormalities consistent with leukoencephalopathy. Finding site True Cerebral white matter structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Early-onset calcifying leucoencephalopathy, skeletal dysplasia Finding site True Cerebral white matter structure Inferred relationship Existential restriction modifier (core metadata concept) 1
PYCR2-related microcephaly, progressive leucoencephalopathy Finding site True Cerebral white matter structure Inferred relationship Existential restriction modifier (core metadata concept) 6
Delayed post-hypoxic leukoencephalopathy Finding site True Cerebral white matter structure Inferred relationship Existential restriction modifier (core metadata concept) 2
White matter disease due to microglioma Finding site True Cerebral white matter structure Inferred relationship Existential restriction modifier (core metadata concept) 1
White matter disease due to anti-phospholipid syndrome (disorder) Finding site True Cerebral white matter structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Toxic leukoencephalopathy (disorder) Finding site True Cerebral white matter structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Stereotactic leucotomy Procedure site - Direct (attribute) True Cerebral white matter structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Adult-onset progressive leukoencephalopathy, early-onset deafness (disorder) Finding site True Cerebral white matter structure Inferred relationship Existential restriction modifier (core metadata concept) 3
A rare neurometabolic disease characterized by acute, reversible, and sometimes recurrent neurologic deterioration (including drowsiness, hypotonia, dysarthria, and ataxia) during a febrile illness. The condition is associated with reversible leukoencephalopathy and persistently increased urinary excretion (and sometimes cerebrospinal fluid concentration) mainly of alpha-ketoglutarate and N-acetylaspartate. Finding site True Cerebral white matter structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Developmental delay, immunodeficiency, leucoencephalopathy, hypohomocysteinemia syndrome Finding site True Cerebral white matter structure Inferred relationship Existential restriction modifier (core metadata concept) 3

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Reference Sets

Lateralizable body structure reference set (foundation metadata concept)

Anatomy structure and entire association reference set (foundation metadata concept)

Anatomy structure and part association reference set (foundation metadata concept)

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